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Severe microcephaly v2.57 SMC1A Arina Puzriakova Phenotypes for gene: SMC1A were changed from Cornelia de Lange syndrome 2, 300590 (includes microcephaly) to Cornelia de Lange syndrome 2, OMIM:300590; Cornelia de Lange syndrome 2, MONDO:0010370; Developmental and epileptic encephalopathy 85, with or without midline brain defects, OMIM:301044; Developmental and epileptic encephalopathy, 85, with or without midline brain defects, MONDO:0026771
Severe microcephaly v1.62 SMC1A Louise Daugherty reviewed gene: SMC1A: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe microcephaly v1.61 SMC1A Louise Daugherty Source NHS GMS was added to SMC1A.
Severe microcephaly SMC1A Rebecca Foulger classified SMC1A as green
Severe microcephaly SMC1A Rebecca Foulger commented on SMC1A
Severe microcephaly SMC1A Rebecca Foulger edited their review of SMC1A
Severe microcephaly SMC1A Rebecca Foulger commented on SMC1A